A novel SLC6A8 mutation associated with motor dysfunction in a child exhibiting creatine transporter deficiency

  1. Cervera-Acedo, C.
  2. Lopez, M.
  3. Aguirre-Lamban, J.
  4. Santibañez, P.
  5. Garcia-Oguiza, A.
  6. Poch-Olive, M.L.
  7. Dominguez-Garrido, E.
Aldizkaria:
Human Genome Variation

ISSN: 2054-345X

Argitalpen urtea: 2015

Alea: 2

Zenbakia: 1

Mota: Artikulua

DOI: 10.1038/HGV.2015.37 GOOGLE SCHOLAR lock_openSarbide irekia editor

Garapen Iraunkorreko Helburuak

Datuen iturria: Scopus